ABSTRACT
We demonstrate a method for measuring the H2 produced in water from the 10B(n,α)7Li fission reaction. Low energy neutrons from the NIST Center for Neutron Research interact with borate-containing water in a temperature-controlled high pressure cell made from titanium. After exposure for one to several hours, the water is extracted and sparged with argon. H2 entrained in the sparging gas is sampled with a small mass spectrometer. To determine the neutron exposure, a small amount of sodium is included in the borate solution. The water is collected and 24Na activation is measured in a counting apparatus on the following day. The G-value for H2 at room temperature is found to be (1.18 ± 0.10) molecules H2/100eV, in good agreement with previous estimates and recent modeling calculations.
ABSTRACT
Molecular hydrogen is a primary product of the interaction of low-LET (γ, ß) radiation with water, and previous measurements have shown that its initial yield increases at elevated temperature. This has been the subject of controversy because more atomic H and (e(-))aq free radicals escape recombination at elevated temperature, and the corresponding production of H2 should decrease. Room temperature experiments have demonstrated that a large fraction of H2 also comes from early physicochemical processes (presumably electron-hole charge recombination and/or dissociative electron attachment), which can be suppressed by scavenging presolvated electrons. In the present work we extend these scavenging measurements up to 350 °C to investigate why the H2 yield increases. We find that most of the H2 yield increase is due to the "presolvation" processes. Relatively small changes in the scavenging efficiency vs LET, and a significant effect of temperature depending on the (positive or negative) charge of the scavenger, indicate that the presolvation H2 is dominated by electron-hole charge recombination rather than dissociative electron attachment at all temperatures.
ABSTRACT
Two copper-uranium heterometallic compounds, [(UO2)3Cu(II)O2(C6NO2)5] (1) and [(UO2)Cu(I)(C6NO2)3] (2), have been synthesized by the reaction of uranyl acetate with copper salts in the presence of isonicotinic acid. Both compounds have been characterized by single-crystal X-ray diffraction, IR, Raman, and UV-vis spectroscopy. In compound 1, interactions between copper and uranium centers occur and result in a three-dimensional pillar layered structure. Compound 1 is also the first example of a heterometallic uranyl organic framework with a trinuclear U3O18 building block. Compound 2 is the first uranyl organic framework that contains monovalent copper, which arises from the reaction of Cu(II) chloride and is assumed to be due to the oxidation of chloride at low pH.
ABSTRACT
Gamma irradiated synthetic hydroxyapatite, bone substituting materials NanoBone(®) and HA Biocer were examined using EPR spectroscopy and compared with powdered human compact bone. In every case, radiation-induced carbon centered radicals were recorded, but their molecular structures and concentrations differed. In compact bone and synthetic hydroxyapatite the main signal assigned to the CO(2) (-) anion radical was stable, whereas the signal due to the CO(3) (3-) radical dominated in NanoBone(®) and HA Biocer just after irradiation. However, after a few days of storage of these samples, also a CO(2) (-) signal was recorded. The EPR study of irradiated compact bone and the synthetic graft materials suggest that their microscopic structures are different. In FT-IR spectra of NanoBone(®), HA Biocer and synthetic hydroxyapatite the HPO(4) (2-) and CO(3) (2-) in B-site groups are detected, whereas in compact bone signals due to collagen dominate.
